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2-(10H-Phenothiazin-10-yl)ethanol, also known as 2-(10-Phenothiazinyl)ethanol or Phenothiazine Ethanol, is a chemical compound with the molecular formula C16H17NOS. It is a derivative of phenothiazine, a heterocyclic compound with a tricyclic structure consisting of two benzene rings and a diazepine ring. 2-(10H-Phenothiazin-10-yl)ethanol is characterized by the presence of an ethanol group (-CH2CH2OH) attached to the phenothiazine nucleus. It is an organic compound that may have potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various phenothiazine-based drugs and dyes. Due to its unique structure, it exhibits specific chemical and physical properties, making it a subject of interest for researchers studying the properties and potential applications of phenothiazine derivatives.

7046-84-6

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7046-84-6 Usage

Chemical structure

Contains a phenothiazine ring and an ethanol functional group.

Common uses

Precursor for the synthesis of other pharmaceutical compounds.

Medical properties

Exhibits antipsychotic, antiemetic, and sedative properties.

Therapeutic applications

Valuable in the treatment of psychiatric and neurological disorders.

Potential uses

Investigated for its use as an antioxidant and in the treatment of certain types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 7046-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7046-84:
(6*7)+(5*0)+(4*4)+(3*6)+(2*8)+(1*4)=96
96 % 10 = 6
So 7046-84-6 is a valid CAS Registry Number.

7046-84-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenothiazin-10-ylethanol

1.2 Other means of identification

Product number -
Other names Phenothiazine-10-ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7046-84-6 SDS

7046-84-6Relevant academic research and scientific papers

A bulge binding agent with novel wedge-shape topology for stimulation of DNA triplet repeat strand slippage synthesis

Liu, Liangliang,Li, Heyang,Yi, Long,Yang, Xing,Wen, Xin,Xi, Zhen

, p. 6184 - 6188 (2008)

Expansion of DNA repeat sequences is associated with many human genetic diseases. Bulged DNA structures have been implicated as intermediates in DNA slippage within the DNA repeat regions. Herein a bulge binding agent with novel wedge-shape topology of the aromatic moiety was designed and synthesized. The compound-bulge DNA interactions were characterized via UV melting experiments, circular dichroism and were quantitated by surface plasmon resonance with Kd of 41.5 μM. This compound showed remarkable stimulation for DNA triplet repeat strand slippage synthesis in vitro.

Well-defined redox-active polymers and block copolymers prepared by living ring-opening metathesis polymerization

Albagli,Bazan,Wrighton,Schrock

, p. 4150 - 4158 (1992)

Mo(CH-t-Bu)(NAr)(O-t-Bu)2 (1a) in THf/0.1 M [n-Bu4N]AsF6 is not oxidized at potentials up to 1.0 V and undergoes a reversible, one electron reduction at -2.16 V vs SCE at a Pt electrode. An analogous intiator containing a

Catalytic Enantioselective Dehydrogenative Si-O Coupling to Access Chiroptical Silicon-Stereogenic Siloxanes and Alkoxysilanes

Zhu, Jiefeng,Chen, Shuyou,He, Chuan

supporting information, p. 5301 - 5307 (2021/05/04)

A rhodium-catalyzed enantioselective construction of triorgano-substituted silicon-stereogenic siloxanes and alkoxysilanes is developed. This process undergoes a direct intermolecular dehydrogenative Si-O coupling between dihydrosilanes with silanols or alocohols, giving access to a variety of highly functionalized chiral siloxanes and alkoxysilanes in decent yields with excellent stereocontrol, that significantly expand the chemical space of the silicon-centered chiral molecules. Further utility of this process was illustrated by the construction of CPL-active (circularly polarized luminescence) silicon-stereogenic alkoxysilane small organic molecules. Optically pure bis-alkoxysilane containing two silicon-stereogenic centers and three pyrene groups displayed a remarkable glum value with a high fluorescence quantum efficiency (glum = 0.011, φF = 0.55), which could have great potential application prospects in chiral organic optoelectronic materials.

Silicon-center chiral silicon-oxygen compound and preparation method thereof

-

Paragraph 0106; 0117; 0119, (2021/07/24)

The invention belongs to the field of chiral silicon synthesis, and discloses a silicon-center chiral silicon-oxygen compound. The compound has a structure represented by general formula I shown in the specification. In the formula I, X is Si(R)n or a formula also shown in the specification, R is selected from alkyl, cycloalkyl and aryl, R is selected from alkyl, substituted phenyl and aryl, R is selected from alkyl, phenyl and substituted phenyl, n is 3, the three R are the same or different, R is selected from hydrogen and (C1-C4) alkyl, m is selected from 0, 1, 2 and 3, and Y is selected from substituted phenyl, substituted pyrenyl, aryl, heteroaryl and cycloalkyl. The invention also discloses a preparation method of the compound. Various highly functionalized chiral siloxanes and silyl ethers are obtained with good chemical, regional and stereo control and high yield, the variety of silicon center chiral compounds is expanded, and the method has the advantages of high enantioselectivity, wide substrate application range, mild reaction conditions, atom economy and the like. In addition, the compound provided by the invention has a huge application prospect in chiral organic photoelectric materials.

Electrical communication between glucose oxidase and electrodes mediated by phenothiazine-labeled poly(ethylene oxide) bonded to lysine residues on the enzyme surface

Ban, Kazumichi,Ueki, Takeshi,Tamada, Yoshinori,Saito, Takahiro,Imabayashi, Shin-ichiro,Watanabe, Masayoshi

, p. 910 - 917 (2007/10/03)

A series of glucose oxidase (GOx) hybrids (GOx-phenothiazine-labeled poly(ethylene oxide) (PT-PEO)) capable of direct electrical communication with electrodes is synthesized by covalently modifying PT-PEO to lysine residues on the enzyme surface. The length of the PEO chain and the number of PT groups are systematically altered. After the PT-PEO modification, all the hybrids maintain more than 50% of enzyme activity relative to that of native GOx, although loss of the activity becomes greater with increasing PEO chain length. The catalytic current, icat, is observed at a potential more positive than 0.55 V after the addition of glucose, due to the intramolecular electron transfer (ET) from reduced forms of flavin adenine dinucletide (FADH2/FADH) to PT+ that are electrogenerated at the electrode. The icat value increases with the number of PT groups, indicating that most of the modified PT groups act as mediators. The magnitude of the icat increase depends on the PEO chain length and reveals a maximum for PT-PEO with the molecular weight of 3000. In contrast, the icat is almost constant for GOx-2-(10-phenothiazyl)propionic acid (PT-PA) hybrids with more than two PT groups synthesized by covalently modifying PT-PA to surface lysines, indicating that only a few key PT groups function as mediators. The maximum rate constant (130 s-1) for the ET from FADH2/FADH to PT+ is obtained for the GOx hybrid modified with five PT-PEO groups with the molecular weight of 3000.

Synthesis and Characterization of Fluorenone-, Anthraquinone-, and Phenothiazine-Labeled Oligodeoxynucleotides: 5′-Probes for DNA Redox Chemistry

Tierney, Mark T.,Grinstaff, Mark W.

, p. 5355 - 5359 (2007/10/03)

A facile and automated procedure for the synthesis of oligodeoxynucleotides possessing derivatives of 9-fluoreneone, 9,10-anthraquinone, and phenothiazine is described. The phosphoramidite approach is used to attach these redox and spectroscopic probes to the 5′-terminus of oligodeoxynucleotides in high yield (>95%). Thermal denaturation studies of labeled oligodeoxynucleotides show a slight enhancement in duplex stability relative to the unlabeled control, and circular dichroism spectra confirm B-form helical DNA structure in solution.

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